Pembrolizumab With or Without Radiation in Patients With Recurrent or Metastatic Adenoid Cystic Carcinoma

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Brief Title

Pembrolizumab With or Without Radiation in Patients With Recurrent or Metastatic Adenoid Cystic Carcinoma

Official Title

A Phase II Trial of Pembrolizumab With or Without Radiation in Patients With Recurrent or Metastatic Adenoid Cystic Carcinoma

Brief Summary

      This research study is studying immunotherapy with or without radiation therapy as a possible
      treatment for adenoid cystic carcinoma.

      The immunotherapy involved in this study is:

        -  Pembrolizumab (MK-3475 or KEYTRUDA).
    

Detailed Description

      This research study is a Phase II clinical trial. Phase II clinical trials test the safety
      and effectiveness of an investigational agent to learn whether it works in treating a
      specific disease. "Investigational" means that the drug is being studied.

      Pembrolizumab (MK-3475 or KEYTRUDA) is a humanized monoclonal antibody. An antibody is a
      common type of protein made in the body in response to a foreign substance (particles not
      typically found in your body such as bacteria or viruses). Antibodies attack foreign
      substances and protect against infection. Antibodies can also be produced in the laboratory
      for use in treating patients. Pembrolizumab is designed to restore the natural ability of the
      immune system to recognize and target cancer cells.

      The FDA recently granted approval to pembrolizumab as a treatment for patients with recurrent
      or metastatic head and neck squamous cell carcinoma. Pembrolizumab has not been approved for
      treatment against adenoid cystic carcinoma.

      This study is testing whether pembrolizumab with or without radiation is useful for patients
      with adenoid cystic carcinoma. Radiation therapy may be used to treat some ACC tumors that
      have spread to other parts of the body or recurred after surgery. Radiation therapy may
      affect the immune system to improve the efficacy of pembrolizumab
    

Study Phase

Phase 2

Study Type

Interventional


Primary Outcome

Objective Response In Non-Irradiated Lesions (Tumor size on scans)

Secondary Outcome

 Progression Free Survival (Time from randomization to disease progression or death)

Condition

Adenoid Cystic Carcinoma

Intervention

Radiation

Study Arms / Comparison Groups

 Pembrolizumab + Radiation
Description:  Up to 5 metastatic lesions targeted with radiation
Over 5 fractions starting within 7 calendar days following the first dose of pembrolizumab
Pembrolizumab will be administered on day 1 of each 21day cycle
Pembrolizumab is delivered intravenously

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information


Recruitment Status

Radiation

Estimated Enrollment

44

Start Date

April 25, 2017

Completion Date

October 31, 2024

Primary Completion Date

December 31, 2020

Eligibility Criteria

        Inclusion Criteria:

          -  Participants must have histologically confirmed adenoid cystic carcinoma with evidence
             of recurrent or metastatic disease not amenable to potentially curative surgery or
             radiotherapy.

          -  Participants must have at least two RECIST v1.1 measurable non-CNS based lesions.
             Palliative radiation must be indicated for at least one of these lesions, and this
             lesion must be a candidate for radiation to a dose of 30 Gy of radiation over 5
             fractions as deemed by a treating radiation oncologist. Documentation of volume and
             prescription isodose line will be collected. Re-irradiation of a previously treated
             lesion is not allowed. One lesion must be in a location where it will not be
             incorporated into the radiation fields so systemic response can be assessed. However,
             inclusion of patients with more than 10 measurable lesions is strongly discouraged and
             all patients must have life expectancy > 6 months.

          -  Participants must agree to undergo a research biopsy, if tumor is safely accessible,
             at baseline and after 2 cycles of pembrolizumab. Participants can be exempt if
             archival tumor tissue has been collected within 12 months of study enrollment that the
             Principal Investigator deems it appropriate/sufficient for analysis on this protocol.
             Biopsy of a lesion outside of the potential radiation treatment field is preferred to
             maintain consistency across cohorts.

          -  Participants must have archival tissue from the primary tumor or metastases available
             for correlative studies. Either a paraffin block or twenty unstained slides are
             acceptable. If twenty slides are not available, a lesser amount may be acceptable
             after discussion with the Principal Investigator.

          -  Prior systemic therapy: At least 2 weeks must have elapsed since the end of prior
             chemotherapy, biological agents (4 weeks for anti-cancer monoclonal antibody
             containing regimens) or any investigational drug product, with adequate recovery of
             treatment-related toxicity to NCI CTCAE Version 4.0 grade ≤1 (or tolerable grade 2) or
             back to baseline (except for alopecia or neuropathy). Any number of prior therapies
             for recurrent/metastatic ACC are allowed, with the exception of previous treatment
             with PD-1 pathway inhibitors.

          -  Prior radiation therapy: At least 3 weeks must have elapsed from prior radiation
             therapy. The prior site of radiotherapy must be documented as reirradiation of the
             same site is not allowed in this protocol.

          -  Be ≥ 18 years of age on day of signing informed consent.

          -  Have a performance status of 0 or 1 on the ECOG Performance Scale (see Appendix A).

          -  Participants must have documentation of a new or progressive lesion on a radiologic
             imaging study performed within 12 months prior to study enrollment (progression of
             disease over any interval is allowed) and/or new/worsening disease related symptoms
             within 12 months prior to study enrollment. This assessment is performed by the
             treating investigator. Evidence of progression by RECIST criteria is not required.

          -  Demonstrate adequate organ function as defined in Table 1, all screening labs should
             be performed within 10 days of treatment initiation.

        Table 1 Adequate Organ Function Laboratory Values System Laboratory Value

          -  Hematological

               -  Absolute neutrophil count (ANC) ≥1,500 /mcL

               -  Platelets ≥100,000 / mcL

               -  Hemoglobin ≥9 g/dL or ≥5.6 mmol/L without transfusion or EPO dependency (within 7
                  days of assessment)

          -  Renal

          -  Serum creatinine OR Measured or calculated creatinine clearance (GFR can also be used
             in place of creatinine or CrCl) ≤1.5 X upper limit of normal (ULN) OR ≥60 mL/min for
             subject with creatinine levels > 1.5 X institutional ULN

          -  Hepatic

               -  Serum total bilirubin ≤ 1.5 X ULN OR Direct bilirubin ≤ ULN for subjects with
                  total bilirubin levels > 1.5 ULN

               -  AST (SGOT) and ALT (SGPT) ≤ 2.5 X ULN OR ≤ 5 X ULN for subjects with liver
                  metastases

               -  Albumin >2.5 mg/dL

          -  Coagulation

               -  International Normalized Ratio (INR) or Prothrombin Time (PT)

               -  Activated Partial Thromboplastin Time (aPTT) ≤1.5 X ULN unless subject is
                  receiving anticoagulant therapy as long as PT or PTT is within therapeutic range
                  of intended use of anticoagulants ≤1.5 X ULN unless subject is receiving
                  anticoagulant therapy as long as PT or PTT is within therapeutic range of
                  intended use of anticoagulants

          -  Creatinine clearance should be calculated per institutional standard.

          -  Baseline tumor measurements must be documented from tests within 28 days of study
             entry. Other non-laboratory tests must be performed within 28 days of study entry.

          -  Female subjects of childbearing potential should have a negative urine or serum
             pregnancy within 7 days prior to receiving the first dose of study medication. If the
             urine test is positive or cannot be confirmed as negative, a serum pregnancy test will
             be required.

          -  Female and male subjects of childbearing potential must agree to use an adequate
             method of contraception, as outlined in section 5.6, prior to study entry, for the
             duration of study participation, and 4 months after completion of pembrolizumab
             administration. Contraception is required starting with the first dose of study
             medication through 120 days after the last dose of study medication.

          -  Note: Abstinence is acceptable if this is the usual lifestyle and preferred
             contraception for the subject.

          -  Be willing and able to provide written informed consent for the trial.

        Exclusion Criteria:

          -  Metastatic disease impinging on the spinal cord or threatening spinal cord
             compression. Patients that have had previous treatment of disease with impinging on
             the cord with either surgery or radiotherapy with clinical or radiographic evidence of
             response or stability are eligible.

          -  Surgical fixation of bone lesion to be irradiated is required and indicated to provide
             mechanical stability.

          -  Participant has known active central nervous system (CNS) metastases and/or
             carcinomatous meningitis. Subjects with previously treated brain metastases may
             participate provided they are stable (without evidence of progression by imaging for
             at least four weeks prior to the first dose of trial treatment), have no evidence of
             new or enlarging brain metastases, and are not using steroids for the purposes of
             treating brain metastasis induced edema for at least 7 days prior to trial treatment.
             This exception does not include carcinomatous meningitis which is excluded regardless
             of clinical stability, because of their poor prognosis and because they often develop
             progressive neurologic dysfunction that would confound the evaluation of neurologic
             and other adverse events.

          -  Prior treatment with PD-1 or PD-L1 inhibitor

          -  Concurrent administration of other cancer specific therapy or investigational agents
             during the course of this study is not allowed.

          -  Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any
             other form of immunosuppressive therapy within 7 days prior to the first dose of trial
             treatment.

          -  Has a known history of active TB (Bacillus Tuberculosis)

          -  History of allergic reactions or hypersensitivity to pembrolizumab or any of its
             excipients.

          -  Uncontrolled intercurrent illness including but not limited to ongoing or active
             infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac
             arrhythmia, or psychiatric illness/social situations that would limit compliance with
             study requirements.

          -  Has a known additional malignancy that is progressing or requires active treatment.
             Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the
             skin that has undergone potentially curative therapy or in situ cervical cancer.

          -  Has known history of, or any evidence of active, non-infectious pneumonitis.

          -  Has an active infection requiring systemic therapy.

          -  Has active autoimmune disease that has required systemic treatment in the past 2 years
             (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive
             drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid
             replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
             form of systemic treatment.

          -  Has a history or current evidence of any condition, therapy, or laboratory abnormality
             that might confound the results of the trial, interfere with the subject's
             participation for the full duration of the trial, or is not in the best interest of
             the subject to participate, in the opinion of the treating investigator.

          -  Subjects who are pregnant or breastfeeding, or expecting to conceive or father
             children within the projected duration of the trial, starting with the pre-screening
             or screening visit through 120 days after the last dose of trial treatment. Pregnant
             women are excluded from this study because immunotherapy has the potential for
             teratogenic or abortifacient effects. Because there is an unknown but potential risk
             of adverse events in nursing infants secondary to treatment of the mother with
             immunotherapy, breastfeeding should be discontinued if the mother is treated on this
             protocol. Women who could potentially become pregnant while undergoing treatment on
             this protocol must be willing to use 2 methods of contraception.

          -  Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).

          -  Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA
             [qualitative] is detected).

          -  Has received a live vaccine within 30 days of planned start of study therapy.
      

Gender

All

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Jonathan Schoenfeld, MD, MPH, , 

Location Countries

United States

Location Countries

United States

Administrative Informations


NCT ID

NCT03087019

Organization ID

16-609


Responsible Party

Principal Investigator

Study Sponsor

Dana-Farber Cancer Institute

Collaborators

 Merck Sharp & Dohme Corp.

Study Sponsor

Jonathan Schoenfeld, MD, MPH, Principal Investigator, Dana-Farber Cancer Institute


Verification Date

July 2020